Ye-qing Qian
1, Xueshi Road
Hangzhou, 310006, China
Hangzhou, 310006, China
Last Updated: 09/26/2026
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Found 17 publications
An efficient molecular genetic testing strategy for incontinentia pigmenti based on single-tube long fragment read sequencing.
Journal: NPJ genomic medicine
Published: October 31, 2023
Clinical Application of Noninvasive Prenatal Testing for Pregnant Women with Assisted Reproductive Pregnancy.
Journal: International journal of women's health
Published: September 01, 2021
Genetic Study and Prenatal Diagnosis of a Family with Thrombocytopenia-Absent Radius (TAR) Syndrome
Journal: Sichuan da xue xue bao. Yi xue ban = Journal of Sichuan University. Medical science edition
Published: July 29, 2021
The association between the two more common genetic causes of spermatogenic failure: a 7-year retrospective study.
Journal: Asian journal of andrology
Published: May 05, 2020
Comprehensive genetic diagnosis of patients with Duchenne/Becker muscular dystrophy (DMD/BMD) and pathogenicity analysis of splice site variants in the DMD gene.
Journal: Journal of Zhejiang University. Science. B
Published: August 06, 2019
Whole-Exome Sequencing Revealed Mutations of MED12 and EFNB1 in Fetal Agenesis of the Corpus Callosum.
Journal: Frontiers in genetics
Published: June 09, 2019
Basonuclin 1 deficiency causes testicular premature aging: BNC1 cooperates with TAF7L to regulate spermatogenesis.
Journal: Journal of molecular cell biology
Published: November 25, 2018
Preimplantation genetic diagnosis and screening (PGD/S) using a semiconductor sequencing platform.
Journal: Human genomics
Published: June 06, 2018
Molecular cloning and expression analysis of a prawn (Macrobrachium rosenbergii) juvenile hormone esterase-like carboxylesterase following immune challenge.
Journal: Fish & shellfish immunology
Published: February 11, 2018
Wntless, a conserved Wnt-transport protein, is involved in the innate immune response of Macrobrachium rosenbergii.
Journal: Fish & shellfish immunology
Published: December 22, 2017
Detection of fetal duplication 16p11.2q12.1 by next-generation sequencing of maternal plasma and invasive diagnosis.
Journal: The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians
Published: September 09, 2017
A feasible diagnostic approach for the translocation carrier from the indication of products of conception.
Journal: Molecular cytogenetics
Published: July 21, 2017
Last Updated: 09/26/2026